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Serum lipids in primary sclerosing cholangitis.

TitleSerum lipids in primary sclerosing cholangitis.
Publication TypeJournal Article
Year of Publication2012
AuthorsSinakos, E., Abbas G., Jorgensen R. A., & Lindor K. D.
JournalDig Liver Dis
Volume44
Issue1
Pagination44-8
Date Published2012 Jan
ISSN1878-3562
KeywordsAdult, Cholangitis, Sclerosing, Cholesterol, Coronary Artery Disease, Female, Follow-Up Studies, Humans, Hyperlipidemias, Lipids, Lipoproteins, Male, Middle Aged, Retrospective Studies, Risk Factors, Stroke, Triglycerides, Ursodeoxycholic Acid
Abstract

BACKGROUND: Limited data are available regarding the serum lipids in primary sclerosing cholangitis.
AIMS: To determine the lipid levels in patients with primary sclerosing cholangitis.
METHODS: We monitored the serum lipid levels annually for up to 6 years in 157 patients included in three previous trials of ursodeoxycholic acid.
RESULTS: The baseline lipid values were: total cholesterol=207 mg/dL (127-433); high-density lipoprotein=56 mg/dL (26-132); low-density lipoprotein=129 mg/dL (48-334); triglycerides=102 mg/dL (41-698). Cirrhotic stage was associated with lower levels of total cholesterol (186 mg/dL vs. 217 mg/dL, p=.02). A significant correlation between the liver biochemistries and total and low-density lipoprotein cholesterol levels was observed. Ursodeoxycholic acid, as compared to placebo, significantly decreased total (-27 mg/dL vs. 22 mg/dL, p=.0004) and low-density lipoprotein cholesterol (-24 mg/dL vs. 17 mg/dL, p=.0001). After extended follow-up, small changes in the lipid levels were noticed. The incidence of coronary artery disease was 4%.
CONCLUSIONS: Our findings suggest that the lipid levels in primary sclerosing cholangitis are often above levels where treatment with lipid-lowering agents is recommended. However, primary sclerosing cholangitis patients seem to have no elevated risk for cardiovascular events. The correlation of total and low-density lipoprotein cholesterol with liver biochemistries implies that mechanisms linked to cholestasis may regulate cholesterol metabolism.

DOI10.1016/j.dld.2011.07.020
Alternate JournalDig Liver Dis
PubMed ID21890438

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